| NDC Code | 68084-749-21 |
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| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-749-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-749-11) |
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| Product NDC | 68084-749 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Losartan Potassium And Hydrochlorothiazide |
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| Non-Proprietary Name | Losartan Potassium And Hydrochlorothiazide |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20140530 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078385 |
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| Manufacturer | American Health Packaging |
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| Substance Name | HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM |
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| Strength | 25; 100 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
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